Canonical Allele Identifier: PA110561
Gene: CYP11A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17523
ClinVar RCV Id: RCV000019075
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000772.2:p.Val415Glu
CA127241
NM_000781.3:c.1244T>A